510(k) K231836 · ODP Intervertebral Fusion Device With Bone Graft, Cervical
ClariVy Cervical IBF System
| Applicant | Vy Spine, LLC, Tallahassee FL, US |
| Decision | Substantially Equivalent, Oct 30, 2023 |
| Received | Jun 22, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231836
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.